Therapeutic Potential of Iron Chelators in Cancer Therapy
- 1 January 2002
- book chapter
- Published by Springer Nature
- Vol. 509, 231-249
- https://doi.org/10.1007/978-1-4615-0593-8_12
Abstract
The development of iron (Fe) chelators for clinical use remains an active research goal. Over the last thirty years desferrioxamine (DFO; DesferalR; Fig. 1) has been the drug of choice in the treatment of Fe overload disease.I’2Despite its considerable success, the problems with this drug remain significant and much research has been invested to obtain alternative ligands (see Chapters 7-9, 13, 14). At present, a number of potential chelators that are orally effective are available for experimental testing (see Chapters 7,13,14). Hence, one can envisage that in the future some of these compounds used alone or in various combinations may provide a better regimen than DFO.Keywords
This publication has 74 references indexed in Scilit:
- Pharmacokinetics and Pharmacodynamics of HydroxyureaClinical Pharmacokinetics, 1998
- Potential of iron chelators as effective antiproliferative agentsCanadian Journal of Physiology and Pharmacology, 1997
- The molecular mechanisms of the metabolism and transport of iron in normal and neoplastic cellsBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1997
- Role of Deferoxamine in Tumor TherapyActa Haematologica, 1996
- Short CommunicationBiological Chemistry Hoppe-Seyler, 1995
- Deferoxamine followed by cyclophosphamide, etoposide, carboplatin, thiotepa, induction regimen in advanced neuroblastoma: Preliminary resultsEuropean Journal Of Cancer, 1995
- The mechanisms of iron uptake by fetal rat hepatocytes in cultureHepatology, 1986
- Site specificity of iron removal from transferrin by α‐ketohydroxypyridine chelatorsFEBS Letters, 1985
- Mobilization of iron from reticulocytesFEBS Letters, 1979
- Nicotinyl and Isonicotinyl Hydrazones of PyridoxalJournal of the American Chemical Society, 1954